Last synced on 14 November 2025 at 11:06 pm

VERITAS Phacoemulsification Console, VERITAS Advanced Fluidics Pack and Advanced Infusion Pack, VERITAS Swivel Handpiece, VERITAS Advanced Foot Pedal, VERITAS Remote Control

Page Type
Cleared 510(K)
510(k) Number
K203060
510(k) Type
Traditional
Applicant
Johnson & Johnson Surgical Vision, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2021
Days to Decision
155 days
Submission Type
Summary

VERITAS Phacoemulsification Console, VERITAS Advanced Fluidics Pack and Advanced Infusion Pack, VERITAS Swivel Handpiece, VERITAS Advanced Foot Pedal, VERITAS Remote Control

Page Type
Cleared 510(K)
510(k) Number
K203060
510(k) Type
Traditional
Applicant
Johnson & Johnson Surgical Vision, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/2021
Days to Decision
155 days
Submission Type
Summary